SNP Links for Gene (Select 100313806) - SNP

Links from Gene

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Select item 14889320811.

rs1488932081 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 4:36427873 (GRCh38)
4:36429495 (GRCh37)
Canonical SPDI:: NC_000004.12:36427872:A:G,NC_000004.12:36427872:A:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000004.12:g.36427873A>G, NC_000004.12:g.36427873A>T, NC_000004.11:g.36429495A>G, NC_000004.11:g.36429495A>T

Select item 14887988002.

rs1488798800 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:36427519 (GRCh38)
4:36429141 (GRCh37)
Canonical SPDI:: NC_000004.12:36427518:T:C
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.36427519T>C, NC_000004.11:g.36429141T>C

Select item 14857701033.

rs1485770103 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:36427181 (GRCh38)
4:36428803 (GRCh37)
Canonical SPDI:: NC_000004.12:36427180:T:G
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000023/6 (TOPMED)
G=0.000312/2 (1000Genomes)
HGVS:: NC_000004.12:g.36427181T>G, NC_000004.11:g.36428803T>G

Select item 14856194584.

rs1485619458 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 4:36427639 (GRCh38)
4:36429261 (GRCh37)
Canonical SPDI:: NC_000004.12:36427638:G:C,NC_000004.12:36427638:G:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.36427639G>C, NC_000004.12:g.36427639G>T, NC_000004.11:g.36429261G>C, NC_000004.11:g.36429261G>T

Select item 14855531485.

rs1485553148 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:36426050 (GRCh38)
4:36427672 (GRCh37)
Canonical SPDI:: NC_000004.12:36426049:A:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000447/2 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000446/2 (Estonian)
HGVS:: NC_000004.12:g.36426050A>T, NC_000004.11:g.36427672A>T

Select item 14855270936.

rs1485527093 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:36426537 (GRCh38)
4:36428159 (GRCh37)
Canonical SPDI:: NC_000004.12:36426536:G:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.36426537G>T, NC_000004.11:g.36428159G>T

Select item 14854436517.

rs1485443651 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:36428130 (GRCh38)
4:36429752 (GRCh37)
Canonical SPDI:: NC_000004.12:36428129:G:A
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000214/3 (ALFA)
A=0.00005/7 (GnomAD)
A=0.00006/16 (TOPMED)
HGVS:: NC_000004.12:g.36428130G>A, NC_000004.11:g.36429752G>A

Select item 14839178718.

rs1483917871 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:36427102 (GRCh38)
4:36428724 (GRCh37)
Canonical SPDI:: NC_000004.12:36427101:G:A
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.36427102G>A, NC_000004.11:g.36428724G>A

Select item 14819135819.

rs1481913581 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:36426822 (GRCh38)
4:36428444 (GRCh37)
Canonical SPDI:: NC_000004.12:36426821:G:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.36426822G>T, NC_000004.11:g.36428444G>T

Select item 147999860510.

rs1479998605 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:36427197 (GRCh38)
4:36428819 (GRCh37)
Canonical SPDI:: NC_000004.12:36427196:C:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.36427197C>T, NC_000004.11:g.36428819C>T

Select item 147921817511.

rs1479218175 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:36427710 (GRCh38)
4:36429332 (GRCh37)
Canonical SPDI:: NC_000004.12:36427709:C:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.36427710C>T, NC_000004.11:g.36429332C>T

Select item 147865918612.

rs1478659186 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:36428160 (GRCh38)
4:36429782 (GRCh37)
Canonical SPDI:: NC_000004.12:36428159:C:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
T=0.000106/2 (TOMMO)
HGVS:: NC_000004.12:g.36428160C>T, NC_000004.11:g.36429782C>T

Select item 147794587913.

rs1477945879 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:36427611 (GRCh38)
4:36429233 (GRCh37)
Canonical SPDI:: NC_000004.12:36427610:G:C
Gene:: MIR1255B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000004.12:g.36427611G>C, NC_000004.11:g.36429233G>C

Select item 147506081914.

rs1475060819 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 4:36427718 (GRCh38)
4:36429340 (GRCh37)
Canonical SPDI:: NC_000004.12:36427717:C:G,NC_000004.12:36427717:C:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000004.12:g.36427718C>G, NC_000004.12:g.36427718C>T, NC_000004.11:g.36429340C>G, NC_000004.11:g.36429340C>T

Select item 147492922915.

rs1474929229 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 4:36427960 (GRCh38)
4:36429582 (GRCh37)
Canonical SPDI:: NC_000004.12:36427959:C:G,NC_000004.12:36427959:C:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.36427960C>G, NC_000004.12:g.36427960C>T, NC_000004.11:g.36429582C>G, NC_000004.11:g.36429582C>T

Select item 147447753216.

rs1474477532 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 4:36425908 (GRCh38)
4:36427530 (GRCh37)
Canonical SPDI:: NC_000004.12:36425903:CACACA:CACA
Gene:: MIR1255B1 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACA=0./0 (ALFA)
-=0.00006/16 (TOPMED)
-=0.000128/18 (GnomAD)
HGVS:: NC_000004.12:g.36425904CA[2], NC_000004.11:g.36427526CA[2]

Select item 147435531417.

rs1474355314 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:36427176 (GRCh38)
4:36428798 (GRCh37)
Canonical SPDI:: NC_000004.12:36427175:C:A,NC_000004.12:36427175:C:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.36427176C>A, NC_000004.12:g.36427176C>T, NC_000004.11:g.36428798C>A, NC_000004.11:g.36428798C>T

Select item 147344536918.

rs1473445369 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:36426901 (GRCh38)
4:36428523 (GRCh37)
Canonical SPDI:: NC_000004.12:36426900:C:A,NC_000004.12:36426900:C:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000064/9 (GnomAD)
HGVS:: NC_000004.12:g.36426901C>A, NC_000004.12:g.36426901C>T, NC_000004.11:g.36428523C>A, NC_000004.11:g.36428523C>T

Select item 147311315719.

rs1473113157 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:36427930 (GRCh38)
4:36429552 (GRCh37)
Canonical SPDI:: NC_000004.12:36427929:C:A,NC_000004.12:36427929:C:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000066/1 (ALFA)
A=0./0 (GnomAD)
HGVS:: NC_000004.12:g.36427930C>A, NC_000004.12:g.36427930C>T, NC_000004.11:g.36429552C>A, NC_000004.11:g.36429552C>T

Select item 146955335420.

rs1469553354 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:36427389 (GRCh38)
4:36429011 (GRCh37)
Canonical SPDI:: NC_000004.12:36427388:C:T
Gene:: MIR1255B1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.36427389C>T, NC_000004.11:g.36429011C>T

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